Home FDA labels 5134aec4-e4a8-4522-9a1d-c3dae8b003fb Pericardium Triple Warmer Meridian Opener openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Pericardium Triple Warmer Meridian Opener
Generic name ARSENICUM ALBUM, AURUM METALLICUM, BARYTA CARBONICA, CALCAREA CARBONICA, GLONOINUM, IODIUM, KALI IODATUM, LACHESIS MUTUS, LITHIUM CARBONICUM, MERCURIUS SOLUBILIS, NAJA TRIPUDIANS, PHOSPHORICUM ACIDUM, PHOSPHORUS, SEPIA, SPONGIA TOSTA, TABACUM, THYROIDINUM (SUIS)
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 060ecfed-5d31-49ca-82d8-9b05355da59d
SPL ID 5134aec4-e4a8-4522-9a1d-c3dae8b003fb
Version 5
Effective date 2024-10-22
Source export date 2026-09-28
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:19:37 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Pericardium Triple Warmer Meridian Opener openfda.brand_name generic name ARSENICUM ALBUM, AURUM METALLICUM, BARYTA CARBONICA, CALCAREA CARBONICA, GLONOINUM, IODIUM, KALI IODATUM, LACHESIS MUTUS, LITHIUM CARBONICUM, MERCURIUS SOLUBILIS, NAJA TRIPUDIANS, PHOSPHORICUM ACIDUM, PHOSPHORUS, SEPIA, SPONGIA TOSTA, TABACUM, THYROIDINUM (SUIS) openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-0652-1 openfda.package_ndc ndc product 43742-0652 openfda.product_ndc ndc11 package 43742065201 derived:openfda.package_ndc spl id 5134aec4-e4a8-4522-9a1d-c3dae8b003fb id spl set id 060ecfed-5d31-49ca-82d8-9b05355da59d set_id unii 27YLU75U4W openfda.unii unii 6RV024OAUQ openfda.unii unii 324Y4038G2 openfda.unii unii QDL83WN8C2 openfda.unii unii 6P669D8HQ8 openfda.unii unii 6YR2608RSU openfda.unii unii 9679TC07X4 openfda.unii unii 79Y1949PYO openfda.unii unii 2E32821G6I openfda.unii unii S7V92P67HO openfda.unii unii VSW71SS07I openfda.unii unii 1C4QK22F9J openfda.unii unii E4GA8884NN openfda.unii unii 1PIP394IID openfda.unii unii G59M7S0WS3 openfda.unii unii ZZ4AG7L7VM openfda.unii unii 2BMD2GNA4V openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: If pregnant of breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.